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Role of MicroRNA-423-5p in posttranscriptional regulation of the intestinal riboflavin transporter-3

机译:MicroRNA-423-5P在肠道核核糖蛋白转运蛋白转运蛋白转运蛋白-3的术后调节作用

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Riboflavin (RF) is essential for normal cellular functions and health. Humans obtain RF from exogenous sources via intestinal absorption that involves a highly specific carrier-mediated process. We have recently established that the riboflavin transporter-3 (RFVT3) is vital for the normal intestinal RF uptake process and have characterized certain aspects of its transcriptional regulation. Little is known, however, about how this transporter is regulated at the posttranscriptional level. We address this issue by focusing on the role of microRNAs. Using bioinformatics, we identified two potential interacting miRNAs with the human (h) RFVT3-3'-UTR, and showed (using pmirGLO-hRFVT3-3'-UTR) that the hRFVT3-3'-UTR is, indeed, a target for miRNA effect. Of the two putative miRNAs identified, miR-423-5p was found to be highly expressed in intestinal epithelial cells and that its mimic affected luciferase reporter activity of the pmirGLO-hRFVT3-3'-UTR construct, and also led to inhibition in RF uptake by intestinal epithelial Caco-2 and HuTu-80 cells. Furthermore, cells transfected with mutated seed sequences for miR-423-5p showed an abrogation in inhibitory effect of the miR-423-5p mimic on luciferase activity. While miR-423-5p did not affect the level of expression of the hRFVT3 mRNA, it did lead to a significant inhibition in the level of expression of its protein. Similarly, miR-423-5p was found to affect the level of expression of the mouse RFVT3 in cultured intestinal enteroids. These findings demonstrate, for the first time, that the RFVT3 is a target for posttranscriptional regulation by miRNAs in intestinal epithelial cells and that this regulation has functional consequences on intestinal RF uptake.
机译:核黄素(RF)对于正常的细胞功能和健康至关重要。人类通过肠道吸收从外源来源获得RF,涉及高度特异性的载体介导的方法。我们最近确定核黄素转运蛋白-3(RFVT3)对于正常肠道RF吸收过程至关重要,并且具有其转录调节的某些方面。然而,众所周知,关于该转运蛋白在后颅面水平时如何调节。我们通过专注于MicroRNA的作用来解决这个问题。使用生物信息学,我们鉴定了具有人(H)RFVT3-3'--UTR的两种潜在的相互作用miRNA,并显示(使用PMIRGLO-HRFVT3-3'--UTR),即,HRFVT3-3'--UTR确实是目标miRNA效应。在鉴定的两个推定的miRNA中,发现MIR-423-5P在肠上皮细胞中高度表达,其模拟受影响的PMIRGLO-HRFVT3-3'-UTR构建体的报告活性,并导致RF摄取中的抑制作用通过肠上皮Caco-2和Hutu-80细胞。此外,用miR-423-5p的突变种子序列转染的细胞显示出在荧光素酶活性上模拟MiR-423-5p的抑制作用的缺失。虽然miR-423-5p不影响HRFVT3 mRNA的表达水平,但它确实导致其蛋白质表达水平的显着抑制。类似地,发现miR-423-5p以影响小鼠RFVT3在培养的肠道内肠骨中的表达水平。这些研究结果首次证明RFVT3是MiRNA在肠上皮细胞中的术语调节的靶标,并且该调节对肠道RF摄取具有功能性后果。

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